Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484167Generated: November 1, 2026

Potassium Carbonate → Methyl 5-[[4,5-dichloro-2-(4-fluoro-2-methoxy-phenoxy)benzoyl]amino]pyridine-2-carboxylate

https://huagongshe.com/reaction/1484167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluoro-2-methoxyphenolHCID 2737368—
ReactantMethyl 5-[(4,5-dichloro-2-fluoro-benzoyl)amino]pyridine-2-carboxylateHCID 90314668—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-[[4,5-dichloro-2-(4-fluoro-2-methoxy-phenoxy)benzoyl]amino]pyridine-2-carboxylateHCID 90315070—

Reaction Conditions

Temperature70 °C

Reaction Steps

Methyl 5-[(4,5-dichloro-2-fluoro-benzoyl)amino]pyridine-2-carboxylate (50 mg, 0.14 mmol), 4-fluoro-2-methoxy-phenol (18.27 μL, 0.16 mmol) and K2CO3 (60.41 mg, 0.44 mmol) were combined in DMF (0.5 mL) and heated at 70° C. for 1.5 hours to form methyl 5-[[4,5-dichloro-2-(4-fluoro-2-methoxy-phenoxy)benzoyl]amino]pyridine-2-carboxylate. Aqueous NaOH (145.7 μL of 3 M, 0.44 mmol) was then added and heating continued for 30 min. HPLC purification (1-99% CH3CN/5 mM HCl) provided 5-(4,5-dichloro-2-(4-fluoro-2-methoxyphenoxy)benzamido)picolinic acid (51) (35.28 mg, 54%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 13.05 (s, 1H), 10.96 (s, 1H), 8.93 (d, J=2.4 Hz, 1H), 8.30 (dd, J=8.7, 2.5 Hz, 1H), 8.08 (d, J=8.6 Hz, 1H), 7.97 (s, 1H), 7.27 (dd, J=8.9, 5.8 Hz, 1H), 7.12 (dd, J=10.7, 2.9 Hz, 1H), 6.91 (s, 1H), 6.84 (td, J=8.5, 2.9 Hz, 1H), 3.75 (s, 3H) ppm. ESI-MS m/z calc. 450.02. found 451.1 (M+1)+; Retention time: 1.61 minutes (3 minutes run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09421196B2
Source datasetuspto-grants-2016_08
ORD IDord-7f15e3855252441c98ddac8183533e51
Source noteuspto-grants-2016_08